Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC

K-Number: K842483 · 1984-08-31

ApplicantSanta Barbara Medco, Inc.
Decision Date1984-08-31
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC is the device name listed in this FDA 510(k) record. The listed applicant is Santa Barbara Medco, Inc.. It received FDA 510(k) clearance on 1984-08-31 under 510(k) number K842483. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC?

SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC is a medical device that received FDA 510(k) clearance on 1984-08-31. The listed applicant is Santa Barbara Medco, Inc.. The 510(k) number is K842483.

When did SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC receive FDA 510(k) clearance?

SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC received FDA 510(k) clearance on 1984-08-31, under 510(k) number K842483.

Who is the listed applicant for SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC?

The FDA 510(k) record lists Santa Barbara Medco, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC?

The FDA product code for SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC is EGJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Santa Barbara Medco, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K850492NASAL SEPTAL BUTTONK823921PHYSICIANS CHOICE SILICONE EAR PUTTYK821187MEDCO CUSTOM EAR PROTECTOR MOLD KITK812069BORES* DEPTH GAUGEK812071RK IV SURGICAL BLADESK812070BORES* ADJUSTABLE BLADE HOLDER

View all 8 devices →

Related Devices (Code: EGJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242041STOPWET iontophoresis apparatus (SW01)Taiwan Medical Electronics Co., Ltd.K241267Hidroxa SE30Hidroxa Medical ABK232020Iontophoresis ElectrodesTop-Rank Health Care Co., Ltd.K192749DermadryDermadry Laboratories, Inc.K191436SaalioSaalmann Medical GmbH & Co. KGK170835Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITEHightech Development

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑